rs104893854

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs104893854(A;A)

Make rs104893854(A;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

4860357

Gene

MSX1

is a	snp
is	mentioned by
dbSNP	rs104893854
dbSNP (classic)	rs104893854
ClinGen	rs104893854
ebi	rs104893854
HLI	rs104893854
Exac	rs104893854
Gnomad	rs104893854
Varsome	rs104893854
LitVar	rs104893854
Map	rs104893854
PheGenI	rs104893854
Biobank	rs104893854
1000 genomes	rs104893854
hgdp	rs104893854
ensembl	rs104893854
geneview	rs104893854
scholar	rs104893854
google	rs104893854
pharmgkb	rs104893854
gwascentral	rs104893854
openSNP	rs104893854
23andMe	rs104893854
SNPshot	rs104893854
SNPdbe	rs104893854
MSV3d	rs104893854
GWAS Ctlg	rs104893854

Max Magnitude

0

OMIM	142983
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104893854(A;A) rs104893854(G;G)
Alt	rs104893854(A;A) rs104893854(G;G)
Reference	Rs104893854(C;C)
Significance	Pathogenic
Disease	Orofacial cleft 5
Variation	info
Gene	MSX1
CLNDBN	Orofacial cleft 5
Reversed	0
HGVS	NC_000004.11:g.4862084C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016014.22,